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慢性阻塞性肺疾病的痰微生物组、气道炎症与死亡率。

The sputum microbiome, airway inflammation, and mortality in chronic obstructive pulmonary disease.

机构信息

the Scottish Centre for Respiratory Research, University of Dundee, Dundee, United Kingdom.

Medical Innovation, GSK R&D, Collegeville, Pa.

出版信息

J Allergy Clin Immunol. 2021 Jan;147(1):158-167. doi: 10.1016/j.jaci.2020.02.040. Epub 2020 Apr 28.

Abstract

BACKGROUND

The sputum microbiome has a potential role in disease phenotyping and risk stratification in chronic obstructive pulmonary disease (COPD), but few large longitudinal cohort studies exist.

OBJECTIVE

Our aim was to investigate the COPD sputum microbiome and its association with inflammatory phenotypes and mortality.

METHODS

16S ribosomal RNA gene sequencing was performed on sputum from 253 clinically stable COPD patients (4-year median follow-up). Samples were classified as Proteobacteria or Firmicutes (phylum level) and Haemophilus or Streptococcus (genus level) dominant. Alpha diversity was measured by using Shannon-Wiener diversity and Berger-Parker dominance indices. Survival was modeled by using Cox proportional hazards regression. A subset of 78 patients had label-free liquid chromatography with tandem mass spectrometry performed, with partial least square discriminant analysis integrating clinical, microbiome, and proteomics data.

RESULTS

Proteobacteria dominance and lower diversity was associated with more severe COPD according to the Global Initiative for Chronic Obstructive Lung Disease classification system (P = .0015), more frequent exacerbations (P = .0042), blood eosinophil level less than or equal to 100 cells/μL (P < .0001), and lower FEV (P = .026). Blood eosinophil counts showed a positive relationship with percent of Firmicutes and Streptococcus and a negative association with percent Proteobacteria and Haemophilus. Proteobacteria dominance was associated with increased mortality compared with Firmicutes-dominated or balanced microbiome profiles (hazard ratio = 2.58; 95% CI = 1.43-4.66; P = .0017 and hazard ratio = 7.47; 95% CI = 1.02-54.86; P = .048, respectively). Integrated omics analysis showed significant associations between Proteobacteria dominance and the neutrophil activation pathway in sputum.

CONCLUSION

The sputum microbiome is associated with clinical and inflammatory phenotypes in COPD. Reduced microbiome diversity, associated with Proteobacteria (predominantly Haemophilus) dominance, is associated with neutrophil-associated protein profiles and an increased risk of mortality.

摘要

背景

痰微生物组在慢性阻塞性肺疾病(COPD)的疾病表型和风险分层中具有潜在作用,但很少有大型纵向队列研究。

目的

我们旨在研究 COPD 痰微生物组及其与炎症表型和死亡率的关系。

方法

对 253 例临床稳定的 COPD 患者(中位随访 4 年)的痰进行 16S 核糖体 RNA 基因测序。样本按变形菌门或厚壁菌门(门水平)和嗜血杆菌属或链球菌属(属水平)优势进行分类。使用 Shannon-Wiener 多样性和 Berger-Parker 优势指数测量 alpha 多样性。使用 Cox 比例风险回归模型对生存进行建模。对 78 例患者进行了无标签液相色谱与串联质谱联用,通过偏最小二乘判别分析整合临床、微生物组和蛋白质组学数据。

结果

根据全球慢性阻塞性肺疾病倡议分类系统,变形菌门优势和多样性降低与 COPD 更严重(P=0.0015)、更频繁的恶化(P=0.0042)、血嗜酸性粒细胞计数小于或等于 100 个/μL(P<0.0001)和 FEV 降低(P=0.026)有关。血嗜酸性粒细胞计数与厚壁菌门和链球菌属的百分比呈正相关,与变形菌门和嗜血杆菌属的百分比呈负相关。与厚壁菌门或平衡微生物组相比,变形菌门优势与死亡率增加相关(风险比=2.58;95%CI=1.43-4.66;P=0.0017 和风险比=7.47;95%CI=1.02-54.86;P=0.048)。综合组学分析显示,变形菌门优势与痰中中性粒细胞激活途径之间存在显著关联。

结论

痰微生物组与 COPD 的临床和炎症表型有关。与变形菌门(主要是嗜血杆菌属)优势相关的微生物组多样性降低与中性粒细胞相关蛋白谱相关,并与死亡率增加相关。

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